SEPT12 mutations cause male infertility with defective sperm annulus

Yung Che Kuo, Ying Hung Lin, Hau Inh Chen, Ya Yun Wang, Yu Wei Chiou, Hsi Hui Lin, Hsien An Pan, Ching Ming Wu, Shih Ming Su, Chao Chin Hsu, Pao Lin Kuo

研究成果: Article同行評審

62 引文 斯高帕斯(Scopus)

摘要

Septins are members of the GTPase superfamily, which has been implicated in diverse cellular functions including cytokinesis and morphogenesis. Septin 12 (SEPT12) is a testis-specific gene critical for the terminal differentiation of male germ cells. We report the identification of two missense SEPT12 mutations, c.266C>T/p.Thr89Met and c.589G>A/p.Asp197Asn, in infertile men. Both mutations are located inside the GTPase domain and may alter the protein structure as suggested by in silico modeling. The p.Thr89Met mutation significantly reduced guanosine-5′-triphosphate (GTP) hydrolytic activity, and the p.Asp197Asn mutation (SEPT12 D197N) interfered with GTP binding. Both mutant SEPT12 proteins restricted the filament formation of the wild-type SEPT12 in a dose-dependent manner. The patient carrying SEPT12 D197N presented with oligoasthenozoospermia, whereas the SEPT12 T89M patient had asthenoteratozoospermia. The characteristic sperm pathology of the SEPT12 D197N patient included defective annulus with bent tail and loss of SEPT12 from the annulus of abnormal sperm. Our finding suggests loss-of-function mutations in SEPT12 disrupted sperm structural integrity by perturbing septin filament formation.

原文English
頁(從 - 到)710-719
頁數10
期刊Human mutation
33
發行號4
DOIs
出版狀態Published - 2012 四月 1

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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